The synthesis of functional derivatives of epoxystearic acid methyl ester by oxirane ring opening and transesterification of ester group has been described. Some novel surface-active and peroxide-containing compounds have been obtained. Major features of the process have been investigated and main characteristics have been determined.
[1] Ray S. and Bousmina M.: Progress in Mat. Sci., 2005, 50, 962.
[2] Tornvall U. and Hatti-Kaul R.: Lipid Techn., 2007, 19, 4.
[3] Knothe G. and Dunn R.: [in:] Gunstone F. and Hamilton R. (Eds.). Oleochemical Manufacture and Applications. Sheffield Academic Press, Sheffield, UK 2001.
[4] Gunstone F.: Biochimica et Biophysica Acta, 2003, 1631, 207.
[5] Warwel S. and Demes C.: Chemosphere, 2001, 43, 39.
[6] Goud V. and Patwardhan A.: Chem. Eng. Sci., 2007, 62, 4065.
[7] Piazza G. and Foglia T.: JAOCS, 2006, 83, 12.
[8] Sepulveda J., Teixeira S. and Schuchard U.: Appl. Catal. A, 2007, 318, 213.
[9] Doll K. and Erhan S.: J. Surfactantsand Detergents, 2006, 9, 4.
[10] Lu J., Khot S. and Wool R.: Polymer, 2005, 46, 71.
[11] Schwetlick K. et al.: [in:] Potapov V. and Ponomarev S (Eds.): Organikum. V. 2. Khimia, Moskwa 1976, 353-377.
[12] Potekhin A.: Svoistva Organicheskih Soedinenij. Spravochnik. Khimia, Leningrad 1984.
[13] Siggia S. and Hanna J.: Quantitative Organic Analysis via Functional Groups. Wiley, New York 1979.
[14] Schwetlick K. et al.: [in:] Potapov V. and Ponomarev S (Eds.): Organikum. V. 2. Khimia, Moskwa 1976, 76-78.
[15] Swern D., Findley T. and Scanlan J.: J. Am. Soc., 1944, 66, 1925.
[16] Belelie et al.: Pat. US 2006/0158491. Publ. July 20, 2006.
[17] Kazicyna L. and Kupletskaya N.: Primenenije UF, IR, NMR-Spectroskopii v Organicheskoj Khimii. Vyshshaja shkola, Moskwa 1971.